화학공학소재연구정보센터
Catalysis Letters, Vol.45, No.3-4, 271-273, 1997
Clay-Catalyzed Radical-Addition of Aliphatic Thiols to Styrene
When placed in K10-montmorillonite and cation-exchanged clays, alkanethiols undergo facile anti-Markovnikov addition to styrene by way of a radical mechanism forming sulfides. Surfactant pillared clays are found to be remarkably selective by suppressing side reactions.